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Ectodermal dysplasia syndrome

MONDO:0019287

The term ''ectodermal dysplasia'' defines a heterogeneous group of heritable disorders of the skin and its appendages characterized by the defective development of two or more ectodermal derivatives, including hair, teeth, nails, sweat glands and their modified structures (i.e. ceruminous, mammary and ciliary glands). The spectrum of clinical manifestations is wide and may include additional manifestations from other ectodermal, mesodermal and endodermal structures.

Also known as: ectodermal dysplasia, ectodermal dysplasia (select examples)

43 clinical trials for this condition and its sub-types.

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Sub-types

Dyskeratosis congenita (12) Cardiofaciocutaneous syndrome (6) Periodontitis, aggressive 1 (6) Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome (4) Papillon-Lefevre disease (4) Hoyeraal-Hreidarsson syndrome (3) Incontinentia pigmenti (3) Odonto-onycho-dermal dysplasia (2) Revesz syndrome (2) Trichothiodystrophy (2) Cardiofaciocutaneous syndrome 1 (1) Cartilage-hair hypoplasia (1) Cronkhite-Canada syndrome (1) Dyskeratosis congenita and related telomere biology disorder (1) Ellis-van Creveld syndrome (1) Hypohidrotic ectodermal dysplasia (1) Trichorhinophalangeal syndrome type II (1) Ackerman syndrome (0) Acrofacial dysostosis, Weyers type (0) ADULT syndrome (0)

Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Syndromic disease (25) Human disease (14) Hereditary skin disorder (6) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Hereditary epidermal appendage anomaly (0)
Trials to join now! 23 Not yet recruiting 2 Not yet finished but already full! 6 Completed 11 Terminated 1
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